Health Enhancement System

ABSTRACT

A health enhancement system establishing a health enhancement program through which may be provided a group of natural products, vitamins and minerals, amino acids, herbs and essential oils that may be helpful in aiding the body in fighting the growth of cancers and the progression of other diseases and in reducing the negative side effects of cancer and cancer treatment, and other diseases and their treatment. At least one embodiment of the invention involves a packaging system of the group of natural products, vitamins and minerals, amino acids, herbs and essential oils that the health enhancement system may comprise.

I. CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a divisional application of U.S. application Ser.No. 10/612,321 filed 1 Jul. 2003, now U.S. Pat. No. 7,273,607, whichclaims the benefit and priority of U.S. Provisional Application60/393,717, filed 1 Jul. 2002, entitled “System for Improving Results ofTreatments and Also for Enhancing an Ability to Resist Certain Types ofDisease”, each said applications hereby incorporated by referenceherein.

II. BACKGROUND

This invention provides a procedure and substances and generally, ahealth enhancement system which can be used to bolster or improve thebody's resistance to certain life threatening conditions such as Cancer,AIDS, Diabetes, Hepatitis, Parkinson's Disease and others. It may beparticularly useful when facing a threat or risk of some cancers inhumans. The system may establish a health enhancement program throughwhich is provided a group of natural products, vitamins and minerals,aminoacids, herbs and essential oils that may be helpful in aiding thebody in fighting the growth of cancers and the progression of otherdiseases and in reducing the negative side effects of cancer and cancertreatment, and other diseases and their treatment(s). It may also assistin slowing, stopping, or reversing the growth of some cancers in theuser. According to one embodiment, the body's ability to achieve aremission of a cancer is believed to be due to its being aided by aunique combination of selected ingredients and dosages. This system may:slow, stop, or reverse the growth of cancerous cells, and/or promotesand strengthen the human bodies own immune defense system against thecancerous cells. Additionally, this system may allow cancer victims tomaintain a significant, higher health status, as defined by mobility,weight gain and energy level during treatment and post treatment. In oneembodiment the ingredients may themselves be significant. In anotherembodiment, the amount, timing and frequency in which the products aretaken may have a significant impact on the treatment performance. Theproducts may also be presented in a unit dose packaging system that mayimprove the patient's ability to accurately follow the use methodologyprescribed. As should be appreciated, the packaging system may also beapplied and used for other administrations as well. In order to trackeffectiveness and/or assure system processes, a set of medical tests maybe required of the patient before and during the course of thetreatment. The tests can be collected and analyzed by the administratoror a health professional to aid in obtaining information on the progressof the patient. There may also be further evidence of the efficacy ofthe products or the system in various cases.

There have been numerous research reports and claim published on theability of natural products, vitamins and minerals to provide eitherenhancements or even effective, alternative means for conventionaltreatments (surgery, chemotherapy and radiation) of some human cancers.Most of this research has focused on the use of one or a limited numberof natural products against a particular type of cancer. Often researchhas been inconclusive with both positive and negative results reported.The present invention provides a new approach to both the products used,the systems followed, and the reporting requirements of a treatmentsystem. It may be applicable in a wide range of treatments; however, itis of particular applicability for a multi-faceted treatment such asproposed to bolster a battle against certain forms of cancer. In oneembodiment, the invention may also be used in combination or conjunctionwith conventional treatments such as surgery, chemotherapy and radiationtherapy. This combination may again provide multiple backups andsynergies that may provide more effective control than any one treatmentor product or therapy. Again, as data is collected (perhaps as part ofthe inventions data collection system) other preferred embodiments mayalso be derived.

III. DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates a unit dose design according to one embodiment.

FIGS. 2-4 each illustrate an embodiment of the packaging system aspectof the invention.

IV. SUMMARY OF THE INVENTION

It is a goal of this invention to provide the cancer patient with acomplement of natural products, vitamins, minerals, amino acids, herbsand essential oils and other ingredients that may directly attack thecancerous cells, which may strengthen and improve the body's own defenseimmune system against cancer, or which may otherwise aid a person in abattle against cancer and other diseases. The present invention providesboth a formulation of ingredients and nutrients for a patient, a systemof use, and a system of administration of such a treatment. It providesfor the proper dosage and accurate ordering by a person in order toassure accuracy of such a potentially complex inter-relation ofpreferably natural substances. In one embodiment, the invention maycontain ingredients that have been selected based on their purportedability by themselves to slow or stop the growth of cancerous cells. Itmay also contain selected levels of vitamins, minerals, and othernutrients that have been determined to enhance the body's naturaldefense systems.

V. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

As can be easily understood, the basic concepts of the present inventionmay be embodied in a variety of ways. It may involve, among otheraspects, a set of ingredients, a series of formulations, a grouping ofdosages, a packaging system, unit dose system, and even a datacollection system in order to accomplish the intended results.

Ingredients:

In one embodiment, the invention's differentiation from othertreatments, in part, may be considered a result of the use ofingredients that when combined provide effects against cancer cells thatmay fall outside of, or in addition to the logical expectation of anysingle ingredient. Many natural products, herbs, vitamins and mineralshave been tested as potential treatments against cancer. Recently, manyresearchers have tested single ingredients, or in some cases,combinations of two or three natural products against specific cancertypes with mixed results. These mixed results may in part be due to thefact that the mechanisms of some various forms of cancer may not be wellunderstood by current science or at least by the researchers. The mixedresults may also be due to some degree by the fact that the researchersmay have been primarily focused on finding a single product oringredient, which is effective against a certain type of cancer.Interrelationships may have been difficult to understand.

In one embodiment, the invention may differ from the singleingredient/specific cancer approach. While the singleingredient/specific cancer approach may provide the most accurateinformation to the researcher on the mechanisms of cancer cell growth,it may do little for the patient who dies if the treatment is noteffective against the type of cancer the patient has. In one embodiment,the invention may be considered as based upon the fact that acombination of ingredients working synergistically may prove to be moreeffective against cancer than any one ingredient by itself. Thisapproach may result in better long-term success rates for cancerpatients than any single ingredient can provide and tests seem toconfirm this aspect.

The present invention includes a variety of ingredients which may beingested in a combined manner in different ways to achieve the intendedresult. At least one embodiment of the health enhancement systemestablishes a 60 day health enhancement program, but certainly programsof other lengths (including non-stop during the life of the programparticipant) should be understood as encompassed by this disclosure.

Each of these ingredients is first discussed separately with a preferredcombination also mentioned. However all the various permutations andcombinations of the individual ingredients should be understood asencompassed by this disclosure.

The invention may be comprised of two subsets of products that whencombined could have the ability to more effectively stop, slow, or evenreverse a growth of cancer cells or to more appropriately enhance thebody's own processes in such a situation. The first subset includesingredients that have been previously reported to individually havespecific, potentially direct effects on cancerous cells as follows:

Shark Cartilage: may inhibit the growth of blood vessels that feedcancerous tumors. This may cut off the nutrition to the tumor andtherefore may not allow the tumor to continue to grow and mutate and totherefore die.Essiac Tea: a four-herb tea developed by an oncology nurse in 1922, thisformula may be excellent for maintaining and healing the liver which isresponsible for detoxifying the blood which may be important in fightingcancer. This formulation may contain burdock root (Arcticum lappa),slippery elm (Ulmus fulva), turkey rhubarb (Rheum palmatum), and sheepsorel (Rumex acetosella). It may also itself serve to kill certaincancer cells. It may be prepared and used as set forth in Table 3. Itmay be important to note that the term essiac tea may refer to theherbal liquid (see Table 3) that may be used to make the preparedbeverage upon dilution of the herbal liquid with warm water.

The following lists a preparation procedure and some use options for theessiac tea feature of the invention.

Table 3

-   -   Preparation of the 4-Herb Formula        -   Supplies Needed:    -   Stainless steel or enamel canning pot (size: 2 gallons or 8        liters) with lid. (Do not use aluminum.)    -   Another large pot to pour hot liquid into while you strain it.        This can be Pyrex or stainless steel.    -   Stainless steel mesh strainer and spoon and ladle (a large soup        serving spoon)16 ounce (⅛ liter) or 32 ounce (¼ liter) amber        glass bottles in which to store your finished product (they        should be amber or a dark color, as the formula is light        sensitive and will not stay as potent in clear glass bottles)

Preparation Procedure:

To make the one gallon recipe, use the four herb-package (approximately½ cup). Bring one gallon of water to a boil. Stir in herbs, replace lidand boil for 10 minutes. Turn off stove, scrape down sides, mix well andallow pot to sit and remain closed for 12 hours.

(This is the Steeping and Extraction Process.)

-   After 12 or more hours, reheat to almost boiling (about 10 minutes).    Let cool for 5 minutes and begin straining process. Strain as many    times as you like. A little herb left in the liquid will not hurt it    in any way. It is also satisfactory to allow the solids, etc. to    settle to the bottom and then skim off the liquid with a soup ladle.    Reheat your liquid once again (2 to 3 minutes only). This will kill    any bacteria that may have landed in your liquid and help keep it    from spoiling.-   Using a funnel or a glass measuring cup, put your hot liquid into    preheated bottles. You can heat the bottles in the oven at 200    degrees for 5 or 10 minutes. Do not put bottle caps in oven!-   Cap, let cool and then put in the refrigerator. This will be good    for one month. Label the bottles the day you make the tea and also    the day it expires.

Usage Directions:

Mix 2 ounces of herbal liquid with two ounces of warm water. Never heatthis formula or the hot water in a microwave!

The formula should be taken on an empty stomach to allow for betterabsorbability. Always take before eating. Wait 15 to 20 minutes beforeeating.

This formula can be taken 1 to 3 times per day. The herbal formula isnon-toxic in proper doses and has a pleasant taste similar to black tea.These herbs do stimulate the body to throw off toxins and, therefore, itis important that you drink plenty of clean water and have regular bowelmovements.

For cancer and serious ailments the dosage is 3 times per day for aslong as tests indicate the presence of cancer. Then 2 times per day foran additional year. For long term maintenance and gentle detoxificationthe dosage is 1 time per day.

Flax Oil: this is a source of linolenic and linoleic acids, which may bevital in providing nutrients to the non-cancer cells. These compoundscontained in flax may also attack the mutating cells in a manner, whichdoes not significantly affect healthy body cells and may not possess thedestructive side effects of conventional chemotherapy.Omega 3 Oil: this is an additional source of linoleic and linolenicacids from certain fish species.Hydrazine Sulfate: used to treat cachexia, and symptoms associated withchemotherapy, such as loss of hair, nausea, pain, weight loss, andgeneral deterioration of vital organs, the body, and muscles. This maybe considered a MAO inhibitor, and may allow the body to toleratechemotherapy while allowing the organ systems to continue the processingof nutrition.Cat's Claw: (Una de Gato) potentially a strong anti-oxidant althoughoften used in central and south America for centuries as a generalwellness product. It may have alkaloids (vinca alkaloids), which mayhave anti-tumor properties much like the chemotherapy drugs Vincristineand Vinblastine; only this nutritional product may be largely free ofthe side effects.

In one embodiment, a goal of this first subset of ingredients may beconsidered as providing multiple, alternative products that are selectedto have some type of anti-cancer cell properties. Since the effects ofeach of the above ingredients on cell growth of the many different typesof cancer may be considered as not totally understood by currentscience, in a general sense, the invention may be considered asproviding multiple backups and synergies that may provide more effectivecontrol than any one or two of the products. As more data is collected(potentially as part of the invention's data collection system), otherpreferred embodiments may be derived. These embodiments may include moreingredients, or fewer, as the results dictate.

The second subset of ingredients can be generally described as naturalproducts, vitamins and minerals that are selected for their positiveeffects on the body's ability to build and maintain a healthy immunedefense system. This subset of ingredients may include the following:

Products sold under the trademark Heritage Complete™ or the like (suchas provided by Heritage Health™ Products): A particularly good multiplevitamin and amino acid and mineral product. This may be selected toprovide the body the basic building blocks of nutritional components tosustain health during the cancer fight and thereafter their ingredients(To the extent composite products such as this are referenced, all eachincorporated by reference herein.), as publicly available.

Products sold under the trademark Dino Bites™ or the like (such asprovided by Heritage Health™ Products): a montmorillonite mineralsupplement used in concert with the above complete multiple vitaminproduct to ensure absorption of the vitamins and to provide more thansixty trace minerals.

Vitamin C: (ascorbic acid ester) a necessary building block to provideenergy for the Krebs cycle as well as an excellent anti-oxidant.

Vitamin A: (beta-carotene) a strong antioxidant that deals directly withand destroys free radicals produced from use of radiation andchemotherapy.

Vitamin E: (d-alpha-tocopherol) another strong antioxidant as well as afacilitator of fat-soluble vitamins. Also responsible for regulation ofblood flow with regard to prevention of blood clots.

Products sold under the trademark Heritage Osteoguard™ or the like (suchas provided by Heritage Health™ Products): a hydroxyadpatite calcium andmagnesium supplement that may ensure the patient has bone strength.Chemotherapy, without a calcium supplement, can remove the requiredcalcium from the bones of the patient, ultimately causing weakness and ageneral sense of malaise.

Products sold under the trademark Heritage Platinum™: (oligomericproanthocyanidins) or the like (such as provided by Heritage Health™Products) may provide strengthened immune function, stimulates T-4killer cell production as well as white blood cell production, which maybe critical to attacking mutated cancer cells. This may serve as anoverall nutritional supplement for the immune system.

Products sold under the trademark Heritage Gold™ or the like (such asprovided by Heritage Health™ Products): a digestive enzyme product,which is critical in the breakdown of food. Often cancer patients areintolerant to retention of food; this may serve to break down the foodand ensure absorption via the small intestine. This product may alsoallow absorption of all of the nutritional supplements listed herein aswell.

In one embodiment, a goal of this second subset of ingredients may be toprovide the body with important nutrients and vitamins that may allowthe body's natural immune defense system to complement the first subsetof ingredients. This may also provide far more effective control of thecancer cells, and may maintain better health in the patient. Because theeffects of each of the above ingredients on the body's natural immunedefense system may also be considered as not totally understood bycurrent science from some perspectives, the invention may again providemultiple backups and synergies that may provide more effective controlthan any one product. Again, as data is collected (perhaps as part ofthe invention's data collection system), other preferred embodiments maybe derived. These embodiments may include more ingredients, or fewer, orsome additional ones, as results dictate.

In one preferred embodiment of the health enhancement system, the dosageand/or timing of the ingredients may be considered important. One suchsystem of dosages and timing is shown in Tables 1 and 2. Importantly, itshould be understood that these dosages and/or timings of the listedingredients are elements of a health enhancement system establishing ahealth enhancement program that, in Tables 1 and 2, is a preferredembodiment as currently understood. Other dosages and timings may proveto be appropriate and may produce satisfactory results and to the extentthe ingredients are disclosed herein, all permutations andcombinations—even of each elements' sub-elements—should be understood asencompassed by this disclosure. Specifically, elimination of one or moreof the ingredients from the system presented in Tables 1 and 2, oralteration of the dosage and/or timing of the ingredients presented inTables 1 and 2 is to be understood as encompassed by this disclosure. Asdata is collected (perhaps as part of the invention's data collectionsystem), other preferred embodiments may be derived. These embodimentsmay include higher or lower dosages of each of the ingredients,separately or in total. It may be important to understand that a dailyportion of any ingredient may be in two or more smaller portions (e.g.,one of which is for ingestion in the morning and the other, in theevening).

TABLE 1 Products and Dosage 1. Flax Oil - 2 capsules (1,000 mg each)each morning and evening. 2. Heritage Omega-3 Oil 1 2 capsules (1,000 mgeach) each morning and evening. 3. Shark Cartilage - 5 capsules (250 mgeach) each morning and evening. 4. Heritage Dino Bites -(montmorillinite minerals) 1 tablet (300 mg) each morning and evening.5. Vitamin C - 2 tablets (500 mg each) each morning and evening. 6. BetaCarotene (Vitamin A) - 1 capsule (25,000 IU) every two days. 7. HeritageComplete - 2 tablets each morning and evening. Each tablet consists ofmultivitamins and minerals:: Vitamin A 1,666 IU Vitamin C 100 mg VitaminD 66 IU Vitamin E 33 IU Vitamin K 13 mcg Thiamin 2.5 mg Riboflavin 2.8mg Niacin 17 mg Vitamin B6 3.3 mg Folic Acid 67 mcg Vitamin B12 10 mcgBiotin 50 mcg Pantothenic Acid 10 mg Calcium proteinate 17 mg Iodine 25mcg Magnesium 17 mg Zinc 2.5 mg Selenium 12 mcg Copper proteinate 0.33mg Manganese 1.7 mg Chromium 34 mcg Molybdenum 17 mcg Potassium 17 mgGarlic Cloves 83 mg Choline 34 mg Inositol 17 mg PABA 17 mg Boron 0.5 mgOctosanol 0.5 mg Silicon 0.17 mg Vanadium 17 mcg Blend: Chlorella,Korean Ginseng, Lemon bioflavenoids, Papain, Rose Hips, Rutin, CoenzymeQ 10. 8. Heritage Osteoguard - 1 tablet each morning and evening. Eachtablet contains: Vitamin D 10 IU Hydroxyadpatite and citrate 250 mgMagnesium (as citrate) 100 mg 9. Heritage Platinum - 2 capsules eachmorning and evening. Each capsule contains: Pine Bark Extract 10 mgGrape Seed Extract 40 mg Blend of citrus bioflavenoids, Rutin, Quercetin10. Heritage Cat's Claw 1 1 capsule (600 mg) each morning and evening11. Heritage Gold - 1 capsule each morning and evening. Each capsulecontains Pancreatin, Lactase, Lipase, Amylase, Catalase, Chrymotrypsin,Trypsin, Cellulase, Zinc Gluconate. 12. Vitamin E - 1 softgel (400 IU)each morning and evening. 13. Essiac Tea - Drink 2 ounces of tea 3 timesdaily at least 20 minutes prior to eating. 14. Hydrazine Sulfate - 60 mgtablets. A. One tablet daily for first three days. B. Two tablets dailyfor days 4, 5, and 6. C. Three tablets daily for the following 46 days.D. No tablets for 7 days.

TABLE 2 Products and Dosage 1. Flax Oil - 2 capsules (1,000 mg each)each morning and evening. 2. Heritage Omega-3 Oil - 2 capsules (1,000 mgeach) each morning and evening. 3. Shark Cartilage - 10 capsules (250 mgeach) each morning and evening. 4. Heritage Dino Bites -(montmorillinite minerals) 1 tablet (300 mg) each morning and evening.5. Vitamin C - 2 tablets (500 mg each) each morning and evening. 6. BetaCarotene (Vitamin A) - 1 capsule (10,000 IU) every morning. 7. HeritageComplete - 3 tablets each morning and evening. Each tablet consists ofmultivitamins and minerals:: Vitamin A 1,666 IU Vitamin C 100 mg VitaminD 66 IU Vitamin E 33 IU Vitamin K 13 mcg Thiamin 2.5 mg Riboflavin 2.8mg Niacin 17 mg Vitamin B6 3.3 mg Folic Acid 67 mcg Vitamin B12 10 mcgBiotin 50 mcg Pantothenic Acid 10 mg Calcium proteinate 17 mg Iodine 25mcg Magnesium 17 mg Zinc 2.5 mg Selenium 12 mcg Copper proteinate 0.33mg Manganese 1.7 mg Chromium 34 mcg Molybdenum 17 mcg Potassium 17 mgGarlic Cloves 83 mg Choline 34 mg Inositol 17 mg PABA 17 mg Boron 0.5 mgOctosanol 0.5 mg Silicon 0.17 mg Vanadium 17 mcg Blend: Chlorella,Korean Ginseng, Lemon bioflavenoids, Papain, Rose Hips, Rutin, CoenzymeQ 10. 8. Heritage Osteoguard - 1 tablet each morning and evening. Eachtablet contains: Vitamin D 10 IU Hydroxyadpatite and citrate 250 mgMagnesium (as citrate) 100 mg 9. Heritage Platinum - 2 capsules eachmorning and evening. Each capsule contains: Pine Bark Extract 10 mgGrape Seed Extract 40 mg Blend of citrus bioflavenoids, Rutin, Quercetin10. Heritage Cat's Claw - 1 capsule (600 mg) each morning and evening11. Heritage Gold - 1 capsule each morning and evening. Each capsulecontains Pancreatin, Lactase, Lipase, Amylase, Catalase, Chrymotrypsin,Trypsin, Cellulase, Zinc Gluconate. 12. Vitamin E - 1 softgel (400 IU)each morning and evening. 13. Essiac Tea - Drink 2 ounces of tea 3 timesdaily at least 20 minutes prior to eating.

In another embodiment, the user may also be encouraged to modify theirdiet in two main ways. First, to greatly reduce fat content to less than25% of total daily caloric intake, especially of saturated fats. Second,to add daily portions of cruciferous vegetables at every meal possible.In combination with other aspects of the invention, the multiplesynergies and backups may provide more effective control than any onetreatment or therapy.

Unit Dose Packaging System

As shown in FIG. 1 the invention may be presented to a user in a unitdose design. The appropriate dose of each ingredient may even bepackaged for sequential use, such as once each morning and evening bythe user. This design may increase the accuracy and timing of the dosingby the patient, and may increase the efficacy. Given the need tomaintain a consistent level of each ingredient in the patient, one goalof this feature of the invention may be to make a complex administrationsystem easier for the patient to take the proper dosage at the correcttimes.

In one preferred embodiment, the proper dosage of each of theingredients may be included as part of a package of ingredients (5) thatcomprises daily portions of a multi-day supply (such as a one week orseven day supply, e.g.) usable in a health enhancement program for useby the patient at the preferred times, e.g., once each morning andevening. However, other dosages and timings may be appropriate to givethe intended result. In this regard, combinations using morning andevening administrations as well as three times per day, four times perday, and even once per day (as but a few examples) should be understoodas encompassed by this disclosure as each may be appropriate in a givencontext. In at least one embodiment, the ingredients are relationallycoordinated in that the type and/or dosage and/or timing is selected tocause a health enhancing effect. Based on the information gatheredthrough the use of the data collection system, dosages and timings ofeach ingredient may even be altered, increased or decreased to maximizethe effectiveness. A rapid feedback process may even be implemented tooptimize effectiveness for each user.

Data Collection System

As a way to assure or perhaps enhance efficacy, and perhaps also as away to encourage usage and even track the effectiveness of theinvention, a data collection system may be implemented. In oneembodiment, certain personal, usage, and/or medical records of thepatient/customer may be collected. One goal of this system may be toinsure that information is gathered which may be necessary to allow theeffectiveness of the invention to be demonstrated, and which may beuseful to consider adjustments made to the ingredients, timing, dosagesand packaging system for maximum effectiveness, and which may be usefulfor marketing purposes. Additionally, this system may serve to encouragethe customer/patient to be under the care of a medical professionalwhich may not only assure optimal care, but it may also enhance theperceptions by the patient and thereby enhance the system'seffectiveness.

In a preferred embodiment, the data collection system may be designed torequire that each patient/customer of a kit produce certain medicalrecords at the time of purchase. These records may include diagnosis,prognosis, list of current medicines, treatment and medical history andother appropriate tests such as blood tests etc. Periodically, thepatient/customer may also be required to update these medical records,such as on a monthly, weekly, bi-weekly, or even bimonthly basis, but atleast at the time of each subsequent sale, in order to track theprogress of their disease and perhaps even determine the propriety ofany additional purchases.

It may be useful to note that the invention and its formulation appearto have produced what may be considered by some to be spectacularresults. Although these results may be considered as only representing alimited test basis, they are significant to those having used the system(including an inventor hereof relative to an advanced case of one of themost deadly forms of cancer, multiple myeloma or bone cancer). Throughthe use of data collected under one embodiment, further analysis of theresults may also be accomplished.

As mentioned earlier, the present invention includes a variety ofaspects, which may be combined in different ways. The followingdescriptions are provided to list elements and describe some of theembodiments of the present invention. These elements are listed withinitial embodiments, however it should be understood that they may becombined in any manner and in any number to create additionalembodiments. The variously described examples and preferred embodimentsshould not be construed to limit the present invention to only theexplicitly described systems, techniques, and applications. Further,this description should further be understood to support and encompassdescriptions and claim of all the various embodiments, systems,techniques, methods, devices, and applications with any number of thedisclosed elements, with each element alone, and also with any and allvarious permutations and combinations of all elements in this or anysubsequent application.

As can be easily understood from the foregoing, the basic concepts ofthe present invention may be embodied in a variety of ways. Theinvention may be considered as involving a combination of ingredients,formulations of the ingredients, timing and dosages of ingredients, aunit dose system, a health enhancement system that establishes a healthenhancement program, a packaging system and the like as well as allcombinations and permutations of these to improve the efficacy oftreatments. It may also include a data collection system to accomplishthe desired result of slowing or stopping the growth of cancer cells orthe disease in humans and other purposes. While some ingredients,formulations, dosing, methods of packaging and a system of datacollection are disclosed, it should be understood that these not onlyaccomplish certain results but also can be varied in a number of ways.Importantly, as to all of the foregoing each and all of these facetsshould be understood to be encompassed by this disclosure.

It involves both health enhancement techniques as well as devices toaccomplish the appropriate and desired enhancement or improvement ofhealth. In this application, the health enhancement techniques aredisclosed as part of the results shown to be achieved by the variousdevices described and as steps which are inherent to utilization. Theyare simply the natural result of utilizing the devices as intended anddescribed. In addition, while some devices are disclosed, it should beunderstood that these not only accomplish certain methods but also canbe varied in a number of ways. Importantly, as to all of the foregoing,all of these facets should be understood to be encompassed by thisdisclosure.

The discussion included in this non-provisional application is intendedto serve as a basic description. The reader should be aware that thespecific discussion may not explicitly describe all embodimentspossible; many alternatives are implicit. It also may not fully explainthe generic nature of the invention and may not explicitly show how eachfeature or element can actually be representative of a broader functionor of a great variety of alternative or equivalent elements. Again,these are implicitly included in this disclosure. Where the invention isdescribed in device-oriented terminology, each element of the deviceimplicitly performs a function. Apparatus claim may not only be includedfor the device described, but also method or process claim may beincluded to address the functions the invention and each elementperforms. Neither the description nor the terminology is intended tolimit the scope of the claim included in this patent application.

It should also be understood that a variety of changes may be madewithout departing from the essence of the invention. Such changes arealso implicitly included in the description. They still fall within thescope of this invention. A broad disclosure encompassing both theexplicit embodiment(s) shown, the great variety of implicit alternativeembodiments, and the broad methods and/or processes and/or systems andthe like are encompassed by this disclosure, in addition to certainnarrower embodiments. With this understanding, the reader should beaware that this disclosure is to be understood to support the claim inthis patent application. It should be understood that the applicant maylater seek examination of, e.g., even broader claim deemed within theapplicant's right.

Further, each of the various elements of the invention and claim mayalso be achieved in a variety of manners. This disclosure should beunderstood to encompass each such variation, be it a variation of anembodiment of any apparatus embodiment, a method or process embodiment,or even merely a variation of any element of these. Particularly, itshould be understood that as the disclosure relates to elements of theinvention, the words for each element may be expressed by equivalentapparatus terms or method terms—even if only the function or result isthe same. Such equivalent, broader, or even more generic terms should beconsidered to be encompassed in the description of each element oraction. Such terms can be substituted where desired to make explicit theimplicitly broad coverage to which this invention is entitled. As butone example, it should be understood that all actions may be expressedas a means for taking that action or as an element which causes thataction. Similarly, each physical element disclosed should be understoodto encompass a disclosure of the action which that physical elementfacilitates. Regarding this last aspect, as but one example, thedisclosure of a “package” should be understood to encompass disclosureof the act of “packaging”—whether explicitly discussed or not—and,conversely, were there effectively disclosure of the act of “packaging”,such a disclosure should be understood to encompass disclosure of a“package” and even a “means for packaging”. Such changes and alternativeterms are to be understood to be explicitly included in the description.

Any acts of law, statutes, regulations, or rules mentioned in thisapplication for patent; or patents, publications, or other referencesmentioned in this application for patent are hereby incorporated byreference. In addition, as to each term used it should be understoodthat unless its utilization in this application is inconsistent withsuch interpretation, common dictionary definitions should be understoodas incorporated for each term and all definitions, alternative terms,and synonyms such as contained in the Random House Webster's UnabridgedDictionary, second edition are hereby incorporated by reference.Finally, all references listed in the list of References To BeIncorporated By Reference In Accordance With The Provisional PatentApplication or other information statement filed with the applicationare hereby appended and hereby incorporated by reference, however, as toeach of the above, to the extent that such information or statementsincorporated by reference might be considered inconsistent with thepatenting of this/these invention(s) such statements are expressly notto be considered as made by the applicant(s).

Thus, the applicant(s) should be understood to have support to claim andmake a statement of invention to at least: i) each of the healthenhancement systems as herein disclosed and described, ii) the relatedmethods disclosed and described, iii) similar, equivalent, and evenimplicit variations of each of these systems and methods, iv) thosealternative designs which accomplish each of the functions shown as aredisclosed and described, v) those alternative designs and methods whichaccomplish each of the functions shown as are implicit to accomplishthat which is disclosed and described, vi) each feature, component, andstep shown as separate and independent inventions, vii) the applicationsenhanced by the various systems or components disclosed, viii) theresulting products produced by such systems or components, ix) eachsystem, method, and element shown or described as now applied to anyspecific field or devices mentioned, x) methods and apparatusessubstantially as described hereinbefore and with reference to any of theaccompanying examples, xi) the various combinations and permutations ofeach of the elements disclosed, and xii) each potentially dependentclaim or concept as a dependency on each and every one of theindependent claim or concepts presented.

With regard to claim whether now or later presented for examination, itshould be understood that for practical reasons and so as to avoid greatexpansion of the examination burden, the applicant may at any timepresent only initial claim or perhaps only initial claim with onlyinitial dependencies. Support should be understood to exist to thedegree required under new matter laws—including but not limited toEuropean Patent Convention Article 123(2) and United States patent Law35 USC 132 or other such laws—to permit the addition of any of thevarious dependencies or other elements presented under one independentclaim or concept as dependencies or elements under any other independentclaim or concept. In drafting any claim at any time whether in thisapplication or in any subsequent application, it should also beunderstood that the applicant has intended to capture as full and broada scope of coverage as legally available. To the extent thatinsubstantial substitutes are made, to the extent that the applicant didnot in fact draft any claim so as to literally encompass any particularembodiment, and to the extent otherwise applicable, the applicant shouldnot be understood to have in any way intended to or actuallyrelinquished such coverage as the applicant simply may not have beenable to anticipate all eventualities; one skilled in the art, should notbe reasonably expected to have drafted a claim that would have literallyencompassed such alternative embodiments.

Further, if or when used, the use of the transitional phrase“comprising” is used to maintain the “open-end” claim herein, accordingto traditional claim interpretation. Thus, unless the context requiresotherwise, it should be understood that the term “comprise” orvariations such as “comprises” or “comprising”, are intended to implythe inclusion of a stated element or step or group of elements or stepsbut not the exclusion of any other element or step or group of elementsor steps. Such terms should be interpreted in their most expansive formso as to afford the applicant the broadest coverage legally permissible.

Finally, any claim set forth at any time are hereby incorporated byreference as part of this description of the invention, and theapplicant expressly reserves the right to use all of or a portion ofsuch incorporated content of such claim as additional description tosupport any of or all of the claim or any element or component thereof,and the applicant further expressly reserves the right to move anyportion of or all of the incorporated content of such claim or anyelement or component thereof from the description into the claim orvice-versa as necessary to define the matter for which protection issought by this application or by any subsequent continuation, division,or continuation-in-part application thereof, or to obtain any benefitof, reduction in fees pursuant to, or to comply with the patent laws,rules, or regulations of any country or treaty, and such contentincorporated by reference shall survive during the entire pendency ofthis application including any subsequent continuation, division, orcontinuation-in-part application thereof or any reissue or extensionthereon.

1-30. (canceled)
 31. A package of ingredients usable in a healthenhancement program, wherein said package of ingredients comprises:daily portions of a seven day supply of each of said ingredients, saidingredients comprising: flax oil; omega-3 oil; shark cartilage;montmorillinite minerals; vitamin C; Heritage Complete™; HeritageOsteoguard™; Heritage Platinum™; Cat's Claw; Heritage Gold™; and vitaminE; and portions of a seven day supply of beta carotene, wherein saidingredients are relationally coordinated to enhance health when ingestedaccording to said health enhancement program.
 32. A package ofingredients usable in a health enhancement program as described in claim31 wherein said package of ingredients further comprises hydrazinesulfate.
 33. A package of ingredients usable in a health enhancementprogram as described in claim 32 wherein: said daily portions of a sevenday supply of flax oil comprise daily portions each in the amount of4,000 mgs.; said daily portions of a seven day supply of omega-3 oilcomprise daily portions each in the amount of 4,000 mgs.; said dailyportions of a seven day supply of shark cartilage comprise dailyportions each in the amount of 1250 mgs.; said daily portions of a sevenday supply of montmorillinite minerals comprise daily portions each inthe amount of 600 mgs.; said daily portions of a seven day supply ofvitamin C comprise daily portions each in the amount of 2000 mgs.; saiddaily portions of a seven day supply of Heritage Complete™ comprisedaily portions each in the amount of four tablets; said daily portionsof a seven day supply of Heritage Osteoguard™ comprise daily portionseach in the amount of two tablets; said daily portions of a seven daysupply of Heritage Platinum™ comprise daily portions each in the amountof four capsules; said daily portions of a seven day supply of Cat'sClaw comprise daily portions each in the amount of 1200 mgs.; said dailyportions of a seven day supply of Heritage Gold™ comprise daily portionseach in the amount of two capsules; said daily portions of a seven daysupply of Vitamin E comprise daily portions each in the amount of 800IU.; said portions of a seven day supply of beta carotene comprisetwo-day portions each in the amount of 25,000 IU; wherein said dailyportions of a seven day supply of hydrazine sulfate comprise an amountappropriate as specified by the following hydrazine schedule: 60 mg.hydrazine sulfate daily for the first three days of administration ofsaid health enhancement program; 120 mgs. hydrazine sulfate daily fordays 4, 5, and 6 of administration of said health enhancement program;180 mgs. hydrazine sulfate daily for days 7 through 52 of administrationof said health enhancement program; and no hydrazine sulfate for days 53through 60 of administration of said health enhancement program.
 34. Apackage of ingredients usable in a health enhancement program asdescribed in claim 31 wherein: said daily portions of a seven day supplyof flax oil comprise daily portions each in the amount of 4,000 mgs.;said daily portions of a seven day supply of omega-3 oil comprise dailyportions each in the amount of 4,000 mgs.; said daily portions of aseven day supply of shark cartilage comprise daily portions each in theamount of 5,000 mgs.; said daily portions of a seven day supply ofmontmorillinite minerals comprise daily portions each in the amount of600 mgs.; said daily portions of a seven day supply of vitamin Ccomprise daily portions each in the amount of 2000 mgs.; said dailyportions of a seven day supply of Heritage Complete™ comprise dailyportions each in the amount of six tablets; said daily portions of aseven day supply of Heritage Osteoguard™ comprise daily portions each inthe amount of two tablets; said daily portions of a seven day supply ofHeritage Platinum™ comprise daily portions each in the amount of fourcapsules; said daily portions of a seven day supply of Cat's Clawcomprise daily portions each in the amount of 1200 mgs.; said dailyportions of a seven day supply of Heritage Gold™ comprise daily portionseach in the amount of two capsules; said daily portions of a seven daysupply of Vitamin E comprise daily portions each in the amount of 800IU.; said portions of a seven day supply of beta carotene comprise dailyportions each in the amount of 10,000 IU.
 35. A package of ingredientsusable in a health enhancement program as described in claim 31, 32, 33or 34 wherein said package of ingredients further comprises essiac tea.36. A package of ingredients usable in a health enhancement program asdescribed in claim 31, 33 or 34 wherein said Omega-3 Oil comprisesHeritage Omega-3 Oil™, wherein said montmorillinite minerals comprisesDino Bites™, wherein said Cat's Claw comprises Heritage Cat's Claw™.